All the information on this site is from our Global Pharmaceutical Database.

sodium fluoride, combinations

North America

Canada (0)
No result.
United States (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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Europe

Austria (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
OTC
-
A01AA51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1-18093
03-06-1986
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Belgium (0)
No result.
Croatia (0)
No result.
Czechia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
33,19MG/G+22,1MG/G 215G
33,19MG/G+22,1MG/G 25G
N
Y
dental
A01AA51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
33,19MG/G+22,1MG/G 215G
33,19MG/G+22,1MG/G 25G
95/ 006/82-S/C
95/ 006/82-S/C
NP
NP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
33,19MG/G+22,1MG/G 215G
33,19MG/G+22,1MG/G 25G
0
0
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Denmark (0)
No result.
Hungary (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
1x215g tube
1x25g tube
N
Y
OTC
OTC
topical
A01AA51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
1x215g tube
1x25g tube
OGYI-T-01646/02
OGYI-T-01646/01
01-01-1991
01-01-1991
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
1x215g tube
1x25g tube
0
0
0
0
0
0
0
0
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Iceland (0)
No result.
Ireland (0)
No result.
Lithuania (0)
No result.
Malta (0)
No result.
Poland (0)
No result.
Romania (0)
No result.
Slovenia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
tubo 215 g gela
tubo 38 g gela
N
-

-
A01AA51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
tubo 215 g gela
tubo 38 g gela
842-25/2019
842-23/2019
-
-
29-01-2019
29-01-2019
29-01-2020
29-01-2020
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
tubo 215 g gela
tubo 38 g gela
21,16
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Spain (0)
No result.
Sweden (0)
No result.
Switzerland (3)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
-
-
D
D
-
A01AA51
-
B
-
A01AA51
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
34916 2
34916 2
Hauptzulassung
Hauptzulassung
17-06-1969
17-06-1969
10-09-2023
10-09-2023
26924 1
Hauptzulassung
02-03-1962
22-01-2022
51226 1
51226 1
Hauptzulassung
Hauptzulassung
09-06-1994
09-06-1994
15-04-2024
15-04-2024
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.